Protease Inhibitors

1.Reactant in preparation of analogs of botulinum neurotoxin serotype A protease inhibitors. 2.Reactant in synthesis of stilbene-based antitumor agents. 3.Reactant in acid-catalyzed preparation of aromatic gem-dihalides from aldehydes and acid

1.Reactant in preparation of analogs of botulinum neurotoxin serotype A protease inhibitors. 2.Reactant in synthesis of stilbene-based antitumor agents. 3.Reactant in acid-catalyzed preparation of aromatic gem-dihalides from aldehydes and acid

1.Reactant in preparation of analogs of botulinum neurotoxin serotype A protease inhibitors. 2.Reactant in synthesis of stilbene-based antitumor agents. 3.Reactant in acid-catalyzed preparation of aromatic gem-dihalides from aldehydes and acid

Indolin-5-amineis a specialty product for proteomics research applications.

A cell-permeable hydroxyethylene dipeptide isostere that acts as a highly specific and a potent inhibitor of &#947-secretase (A&#946 total IC 50 = 17 nM, A&#946 40 IC 50 = 48 nM, and A&#946 42 IC 50 = 67 nM in SHSY5Y cells overexpressing

A cell-permeable hydroxyethylene dipeptide isostere that acts as a highly specific and a potent inhibitor of &#947-secretase (A&#946 total IC 50 = 17 nM, A&#946 40 IC 50 = 48 nM, and A&#946 42 IC 50 = 67 nM in SHSY5Y cells overexpressing

Amino Acid Sequence Z-Leu-Leu-Leu-al General description Potent, reversible, and cell-permeable proteasome inhibitor (K i = 4 nM). Reduces the degradation of ubiquitin-conjugated proteins in mammalian cells and permeable stains of yeast by the 26S

Amino Acid Sequence Z-Leu-Leu-Leu-al General description Potent, reversible, and cell-permeable proteasome inhibitor (K i = 4 nM). Reduces the degradation of ubiquitin-conjugated proteins in mammalian cells and permeable stains of yeast by the 26S

Potent, reversible, and cell-permeable proteasome inhibitor (K i = 4 nM). Reduces the degradation of ubiquitin-conjugated proteins in mammalian cells and permeable stains of yeast by the 26S complex without affecting its ATPase or isopeptidase

Iodo-PEG7-alcohol is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.Appearance:LiquidIC50&amp: Target:PEGsIn Vitro:PROTACs contain two different ligands connected by a linker: one is a ligand for an E3 ubiquitin ligase and

Iodo-PEG7-alcohol is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.Appearance:LiquidIC50&amp: Target:PEGsIn Vitro:PROTACs contain two different ligands connected by a linker: one is a ligand for an E3 ubiquitin ligase and

Iodo-PEG7-alcohol is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.Appearance:LiquidIC50&amp: Target:PEGsIn Vitro:PROTACs contain two different ligands connected by a linker: one is a ligand for an E3 ubiquitin ligase and